The nonlinear interaction of molecules with intense laser fields is a poten
tial method of preparing states with very high degrees of alignment. The ph
ysical rotation of molecules can be confirmed using two pulses of orthogona
l polarization and by observing the behaviour of the lowest fragmentation c
hannels. New results show that this dynamic alignment is molecule specific.
In the case of H-2, virtually all molecules are depleted by the pump pulse
, but we see no evidence for rotation of I-2, in agreement with recent syst
ematic studies of angular distributions. Further analysis indicates that th
e ubiquity of laser-induced alignment has thus far been overestimated.